RecruitingNot ApplicableNCT06189313

CLEANer Aspiration for Pulmonary Embolism

A Prospective, Multicenter Study to Evaluate the Safety and Efficacy of an Aspiration Thrombectomy System in Acute Pulmonary Embolism


Sponsor

Argon Medical Devices

Enrollment

125 participants

Start Date

Jan 3, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

To evaluate the safety and efficacy of the Cleaner™ Pro Thrombectomy System for aspiration thrombectomy in patients with acute pulmonary embolism (PE).


Eligibility

Min Age: 18 Years

Inclusion Criteria5

  • At least 18 years of age at the time of consent
  • Clinical signs, symptoms, and presentation consistent with acute PE
  • Onset of PE symptoms occurred within 14 days of presentation
  • Filling defect in at least one main or lobar pulmonary artery evidenced by CTA
  • RV dysfunction on CTA or echocardiography defined as RV/LV ratio \>0.9

Exclusion Criteria26

  • tPA use within 14 days prior to baseline CTA
  • Systolic BP \<90 mmHg for 15 min or the requirement of inotropic support to maintain systolic BP ≥90 mmHg
  • Diagnosis of pulmonary hypertension primary type I or CTEPH; if patient does not have diagnosis of pulmonary hypertension but peak PA \>70 mmHg by right heart catheterization or elevated main pulmonary artery to aorta ratio (MPA:A), up to investigator discretion.
  • History of severe or chronic pulmonary hypertension
  • FiO2 requirement \>40% or \>6 LPM to keep oxygen saturations \>90%
  • Hematocrit \<28%
  • Platelets \<100,000/µL
  • Serum creatinine \>1.8 mg/dL
  • INR \>3
  • aPTT (or PTT) \>50 seconds on no anticoagulation
  • History of heparin-induced thrombocytopenia (HIT)
  • Recent (within six months) history of stroke, transient ischemic attack (TIA), or intracranial bleeding
  • Recent (within one month) history of active bleeding from a major organ
  • Absolute contraindication to anticoagulation
  • Major trauma such as head trauma, or other active intracranial, or intraspinal disease within 14 days
  • Presence of intracardiac lead in the right ventricle or right atrium placed within 6 months
  • Cardiovascular or pulmonary surgery within last 7 days
  • Cancer which requires active chemotherapy
  • Known serious, uncontrolled sensitivity to radiographic agents
  • Life expectancy \<90 days, as determined by investigator
  • Female who is pregnant
  • Intracardiac thrombus
  • Patients who present with cardiac arrest and/or are on extracorporeal membrane oxygenation (ECMO) or ECMO required to perform interventional procedure
  • Simultaneous participation in another investigational study
  • Patients with known coagulation disorders such as antiphospholipid, Protein C, and Protein S
  • Presentation of PE with paradoxical emboli which may be diagnosed by concurrent stroke or concurrent arterialization

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Interventions

DEVICECleaner Pro Thrombectomy System

The Cleaner™ Pro Thrombectomy System ("Cleaner Pro") is a catheter-based aspiration thrombectomy device comprised of a handpiece, an aspiration catheter, a dilator, and an aspiration canister.


Locations(14)

University of Colorado Anschutz Medical Campus

Aurora, Colorado, United States

Medstar Health Research Institute

Washington D.C., District of Columbia, United States

Ascension Sacred Heart Hospital

Pensacola, Florida, United States

BayCare Health System

Tampa, Florida, United States

Insight Hospital and Medical Center

Chicago, Illinois, United States

Ascension St. Vincent Hospital

Indianapolis, Indiana, United States

UMass Chan Medical School

Worcester, Massachusetts, United States

University Medical Center of Southern Nevada

Las Vegas, Nevada, United States

University of Cincinnati

Cincinnati, Ohio, United States

Cleveland Clinic

Cleveland, Ohio, United States

Promedica Toledo Hospital

Toledo, Ohio, United States

Ascension St. John Jane Phillips Medical Center

Bartlesville, Oklahoma, United States

Baylor Scott and White Heart and Vascular Hospital - Dallas

Dallas, Texas, United States

Baylor Scott & White The Heart Hospital - Plano

Plano, Texas, United States

View Full Details on ClinicalTrials.gov

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NCT06189313


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